Retinal functional change caused by adenoviral vector-mediated transfection of LacZ gene

Human Gene Therapy

Volumn 9, Issue 6, 1998, Pages 789-799

  Sakamoto, Taiji ^a   Ueno, Hikaru ^a   Goto, Yoshinobu ^a   Oshima, Yuji ^a   Yamanaka, Ichiro ^a   Ishibashi, Tatsuro ^a   Inomata, Hajime ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN; GLIAL FIBRILLARY ACIDIC PROTEIN; PROTEIN S 100;

ADENOVIRUS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BACTERIAL GENE; CONTROLLED STUDY; ELECTRORETINOGRAM; GENE EXPRESSION; GENE THERAPY; GENE TRANSFER; GENETIC TRANSFECTION; IMMUNOHISTOCHEMISTRY; NONHUMAN; PIGMENT EPITHELIUM; RAT; RETINA; RETINA CELL;

ADENOVIRIDAE; ANIMALIA; BACTERIA (MICROORGANISMS);

EID: 0032503015     PISSN: 10430342     EISSN: None     Source Type: Journal    
DOI: 10.1089/hum.1998.9.6-789     Document Type: Article

References (8)

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2. BENNETT, J., WILSON, J., SUN, D., FORBES, B., and MAGUIRE, A. (1994). Adenovirus vector-mediated in vivo gene transfer into adult murine retina. Invest. Ophthalmol. Vis. Sci. 35, 2535-2542.
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7. YAMAMOTO, H., UENO, H., OOSHIMA, A., and TAKESHITA, A. (1996). Adenovirus-mediated transfer of a truncated transforming growth factor-β (TGF-β) type II receptor completely and specifically abolishes diverse signaling by TGF-β in vascular wall cells in primary culture. J. Biol. Chem. 271, 16253-16259.
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